918799-14-1

Basic information

• Product Name: 3-Bromo-4,5,6-trimethoxy-2-methylphenol
• Synonyms: 3-Bromo-4,5,6-trimethoxy-2-methylphenol;3-BroMo-4,5,6-triMet
• CAS NO: 918799-14-1
• Molecular Formula: C₁₀H₁₃BrO₄
• Molecular Weight: 277.113
• Mol File: 918799-14-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 345.3 °C at 760 mmHg
• Flash Point: 162.6°C
• Appearance: /
• Density: 1.440
• Vapor Pressure: 3.12E-05mmHg at 25°C
• Refractive Index: 1.543
• CAS DataBase Reference: 3-Bromo-4,5,6-trimethoxy-2-methylphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Bromo-4,5,6-trimethoxy-2-methylphenol(918799-14-1)
• EPA Substance Registry System: 3-Bromo-4,5,6-trimethoxy-2-methylphenol(918799-14-1)

Safety Data

• Hazardous Substances Data: 918799-14-1(Hazardous Substances Data)

Usage

General Description

3-Bromo-4,5,6-trimethoxy-2-methylphenol is a chemical compound with the molecular formula C10H13BrO4. It is a derivative of phenol and contains a bromine atom, three methoxy groups, and a methyl group. 3-Bromo-4,5,6-trimethoxy-2-methylphenol is commonly used in organic synthesis and pharmaceutical research. It has been studied for its potential antioxidant and antimicrobial properties, making it a potentially valuable ingredient in the development of various pharmaceutical and cosmetic products. Additionally, it has been investigated for its potential use in the treatment of various diseases and conditions, making it a compound of interest in the medical and scientific communities.

InChI:InChI=1/C10H13BrO4/c1-5-6(11)8(13-2)10(15-4)9(14-3)7(5)12/h12H,1-4H3

Upstream product

• 39068-88-7 2,3,4-trimethoxy-6-methylphenol 

Downstream Products

• 918799-15-2 2,3,4-trimethoxy-5-bromo-6-methylhydroquinone methoxyethoxymethyl ether 

Relevant articles and documents

Novel Intermediates Useful for the Preparation of Coenzymes, Process for the Preparation of Novel Intermediates and an Improved Process for the Preparation of Coenzymes

The present invention relates to novel intermediates for the preparation of coenzymes, processes for the preparation of the intermediates and an improved process for the preparation of Coenzymes. The present invention particularly relates to an improved process for the preparation of Coenzyme Q, more particularly for Conenzyme Q9 and Coenzyme Q10. Still more particularly this invention relates to regio and stereo controlled process for the preparation of Coenzyme Q9 and Coenzyme Q10 of the formula I where n=9 (Coenzyme CoQ9), and where n=10. (Coenzyme CoQ10)